DOMOIC ACID - A DEMENTIA-INDUCING EXCITOTOXIC FOOD POISON WITH KAINIC ACID RECEPTOR SPECIFICITY

被引:136
作者
STEWART, GR [1 ]
ZORUMSKI, CF [1 ]
PRICE, MT [1 ]
OLNEY, JW [1 ]
机构
[1] WASHINGTON UNIV, SCH MED, DEPT PSYCHIAT, ST LOUIS, MO 63110 USA
关键词
D O I
10.1016/0014-4886(90)90057-Y
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Domoic acid (Dom), a rigid analog of the excitotoxic amino acids, glutamate and kainic acid, is believed to be the mussel neurotoxin responsible for a recent food poisoning incident in Canada that killed some people and left others with memory impairment. Since the literature contains very little information pertaining to Dom excitotoxicity, we have systematically evaluated the neuroexcitatory properties of Dom in vitro (cultured hippocampal neurons) and its neurotoxic properties both in vitro (chick embryo retina) and in vivo (adult rat). In the in vitro experiments, the properties of Dom were compared with those of kainic acid, N-methyl-d-aspartate (NMDA) and quisqualate, each of which is a prototypic agonist at a different subtype of glutamate receptor. Currents induced in hippocampal neurons by Dom and kainic acid were identical and displayed a linear current/voltage relationship (in contrast to NMDA currents) and were nondesensitizing (in contrast to quisqualate currents). Dom currents were not blocked by NMDA antagonists but were blocked by CNQX, an antagonist of non-NMDA receptors. In the chick embryo retina, Dom induced a lesion pattern having the same distinctive characteristics as a kainic acid lesion which differs from that induced by either NMDA or quisqualate, and the Dom lesion was blocked by CNQX but not by NMDA antagonists. Subcutaneous administration of Dom (2.5-3 mg/kg) to adult rats resulted in an acute seizure-brain damage syndrome almost identical to that induced in rats by KA (12 mg/kg) and having important features analogous to the neurotoxic syndrome observed in the human food poison victims. © 1990.
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页码:127 / 138
页数:12
相关论文
共 36 条
[1]  
[Anonymous], KAINIC ACID TOOL NEU
[2]   ELECTROGRAPHIC, CLINICAL AND PATHOLOGICAL ALTERATIONS FOLLOWING SYSTEMIC ADMINISTRATION OF KAINIC ACID, BICUCULLINE OR PENTETRAZOLE - METABOLIC MAPPING USING THE DEOXYGLUCOSE METHOD WITH SPECIAL REFERENCE TO THE PATHOLOGY OF EPILEPSY [J].
BENARI, Y ;
TREMBLAY, E ;
RICHE, D ;
GHILINI, G ;
NAQUET, R .
NEUROSCIENCE, 1981, 6 (07) :1361-1391
[3]  
BISCOE TJ, 1976, BRIT J PHARMACOL, V58, P373, DOI 10.1111/j.1476-5381.1976.tb07714.x
[4]   NEUROTOXICITY AND LETHALITY OF TOXIC EXTRACTS FROM ATLANTIC COAST SHELLFISH [J].
BOSE, R ;
GLAVIN, GB ;
PINSKY, C .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 1989, 13 (3-4) :559-562
[5]   KETAMINE, PHENCYCLIDINE, AND MK-801 PROTECT AGAINST KAINIC ACID-INDUCED SEIZURE-RELATED BRAIN-DAMAGE [J].
CLIFFORD, DB ;
OLNEY, JW ;
BENZ, AM ;
FULLER, TA ;
ZORUMSKI, CF .
EPILEPSIA, 1990, 31 (04) :382-390
[6]   KETAMINE AND MK-801 PREVENT DEGENERATION OF THALAMIC NEURONS INDUCED BY FOCAL CORTICAL SEIZURES [J].
CLIFFORD, DB ;
ZORUMSKI, CF ;
OLNEY, JW .
EXPERIMENTAL NEUROLOGY, 1989, 105 (03) :272-279
[7]   THE FUNCTIONAL-ANATOMY AND PATHOLOGY OF LITHIUM PILOCARPINE AND HIGH-DOSE PILOCARPINE SEIZURES [J].
CLIFFORD, DB ;
OLNEY, JW ;
MANIOTIS, A ;
COLLINS, RC ;
ZORUMSKI, CF .
NEUROSCIENCE, 1987, 23 (03) :953-968
[8]  
Collins R C, 1983, Adv Neurol, V34, P277
[9]   FOCAL CORTICAL SEIZURES CAUSE DISTANT THALAMIC LESIONS [J].
COLLINS, RC ;
OLNEY, JW .
SCIENCE, 1982, 218 (4568) :177-179
[10]   DOMOIC ACID, THE ALLEGED MUSSEL TOXIN, MIGHT PRODUCE ITS NEUROTOXIC EFFECT THROUGH KAINATE RECEPTOR ACTIVATION - AN ELECTROPHYSIOLOGICAL STUDY IN THE RAT DORSAL HIPPOCAMPUS [J].
DEBONNEL, G ;
BEAUCHESNE, L ;
DEMONTIGNY, C .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1989, 67 (01) :29-33